Unknown

Dataset Information

0

Occurrence, function and evolutionary origins of '2A-like' sequences in virus genomes.


ABSTRACT: 2A is an oligopeptide sequence mediating a ribosome 'skipping' effect, producing an apparent 'cleavage' of polyproteins. First identified and characterized in picornaviruses, '2A-like' sequences are found in other mammalian viruses and a wide range of insect viruses. Databases were analysed using a motif conserved amongst 2A/2A-like sequences. The newly identified 2A-like sequences (30 aa) were inserted into a reporter polyprotein to determine their cleavage activity. Our analyses showed that these sequences fall into two categories. The majority mediated very high (complete) cleavage to separate proteins and a few sequences mediated cleavage with lower efficiency, generating appreciable levels of the uncleaved form. Phylogenetic analyses of 2A-like sequences and RNA-dependent RNA polymerases (RdRps) indicated multiple, independent, acquisitions of these sequences at different stages during virus evolution. Within a virus family, 2A sequences are (probably) homologous, but diverge due to other evolutionary pressures. Amongst different families, however, 2A/2A-like sequences appear to be homoplasic.

SUBMITTER: Luke GA 

PROVIDER: S-EPMC2885027 | biostudies-literature | 2008 Apr

REPOSITORIES: biostudies-literature

altmetric image

Publications

Occurrence, function and evolutionary origins of '2A-like' sequences in virus genomes.

Luke Garry A GA   de Felipe Pablo P   Lukashev Alexander A   Kallioinen Susanna E SE   Bruno Elizabeth A EA   Ryan Martin D MD  

The Journal of general virology 20080401 Pt 4


2A is an oligopeptide sequence mediating a ribosome 'skipping' effect, producing an apparent 'cleavage' of polyproteins. First identified and characterized in picornaviruses, '2A-like' sequences are found in other mammalian viruses and a wide range of insect viruses. Databases were analysed using a motif conserved amongst 2A/2A-like sequences. The newly identified 2A-like sequences (30 aa) were inserted into a reporter polyprotein to determine their cleavage activity. Our analyses showed that th  ...[more]

Similar Datasets

| S-EPMC5461048 | biostudies-literature
| S-EPMC4410669 | biostudies-literature
| S-EPMC8623073 | biostudies-literature
| S-EPMC1395342 | biostudies-literature
| S-EPMC4679062 | biostudies-literature
| S-EPMC4442499 | biostudies-literature
| S-EPMC8279507 | biostudies-literature
| S-EPMC6336861 | biostudies-literature
| S-EPMC4729200 | biostudies-literature
| S-EPMC3758194 | biostudies-literature